Flexible cpap mask

ABSTRACT

A respiratory interface device includes a respiratory mask that interfaces with a face of a patient. The respiratory mask comprises a body portion that forms an enclosure around a nose of a patient and at least one set of headgear strap flanges. The body portion is substantially entirely manufactured from an elastomeric material. A bellows-like structure is integrally molded in the body portion to create a sealing interface between an inner bottom portion of the mask and the patient&#39;s nose.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a Divisional of Co-Pending application Ser. No.11/184,370, filed on Jul. 19, 2005, which claims priority to U.S. PatentApplication Ser. No. 60/589,319, filed on Jul. 20, 2004.

FIELD OF THE INVENTION

The present invention relates generally to ventilation devices, and moreparticularly, to a flexible mask for use in a continuous positive airwaypressure system.

BACKGROUND OF THE INVENTION

Sleep apnea is a potentially life-threatening breathing disordercharacterized by brief interruptions of breathing during sleep. Thereare two types of sleep apnea: central and obstructive. Central sleepapnea, which is less common, occurs then the brain fails to sendappropriate signals to the breathing muscles to initiate respirations.Obstructive sleep apnea occurs when air cannot flow into or out of theperson's nose or mouth although efforts to breathe continue. In a givennight, the number of involuntary breathing pauses or “apneic events” maybe as high as 20 to 60 or more per hour. Sleep apnea can also becharacterized by choking sensations. The frequent interruptions of deep,restorative sleep often leads to excessive daytime sleepiness and may beassociated with an early morning headache. Early recognition andtreatment of sleep apnea is important because it may be associated withirregular heartbeat, high blood pressure, heart attack, and stroke.

Various forms of positive airway pressure during sleep can be aneffective form of therapy for the apnea sufferer. Ventilation can beapplied in the form of continuous positive airway pressure (CPAP), inwhich positive pressure is maintained in the airway throughout therespiratory cycle; bi-level positive airway pressure system, in whichpositive pressure is maintained during inspiration but reduced duringexpiration; and intermittent (non-continuous) positive pressure (IPPB),in which pressure is applied when an episode of apnea is sensed. In suchprocedures, a patient wears a mask over the nose during sleep, andpressure from an air blower forces air through the nasal passages.Typically, such masks receive a gas supply line that delivers gas into achamber formed by wall of the mask and the patient's face. The walls areusually semi-rigid and have a face-contacting portion include anaperture that is aligned with the patient's nostrils. Theface-contacting portion can include a soft, resilient elastomericmaterial that can conform to various facial contours. The mask isnormally secured to the patient's head by straps. The straps areadjusted to pull the mask and the patient's face but not so tight as tobe uncomfortable. Gas is thus delivered to the mask and into thepatient's nasal passages.

Problems often arise with masks of the above configuration. For example,the face-contacting portion may apply excessive pressure to the wearer'sface resulting in discomfort and possibly skin irritation. This canoccur because the face-contacting portion has to distort beyond itsnormal range of elasticity to conform to certain facial contours, whichrequires the application of excessive forces. In some cases thesesexcessive pressures and forces may cause the face to distort to conformto the face-contacting portion, which can increase wearer discomfort,resulting in facial soreness and ulceration.

SUMMARY OF THE INVENTION

The following presents a simplified summary of the invention in order toprovide a basic understanding of some aspects of the invention. Thissummary is not an extensive overview of the invention. It is intended toneither identify key or critical elements of the invention nor delineatethe scope of the invention. Its sole purpose is to present some conceptsof the invention in a simplified form as a prelude to the more detaileddescription that is presented later.

The present invention relates to a ventilation interface for acontinuous positive airway pressure system. According to a first aspectof the present invention, an interface device includes a respiratorymask, which comprises a body adapted to form an enclosure around a noseof a patient, wherein the entire body is manufactured from anelastomeric material; and a bellows-like structure integrally molded ina mustache region of the body.

According to another aspect of the present invention, a respiratory maskis provided. The respiratory mask includes an elastomeric body; abellows-like structure integrally molded in a mustache region of thebody; and at least one headgear strap flange integrally molded with thebody.

According to yet another aspect of the present invention, a respiratorymask is provided. The respiratory mask comprises elastomeric mask meansfor forming an enclosure around a nose of a patient; and bellowsintegrally molded in the mask means for creating a sealing interfacebetween an inner bottom portion of the mask means and a bottom portionof a patient's nose.

The following description and the annexed drawings set forth in detailcertain illustrative aspects of the invention. These aspects areindicative, however, of but a few of the various ways in which theprinciples of the invention may be employed and the present invention isintended to include all such aspects and their equivalents. Otherobjects, advantages and novel features of the invention will becomeapparent from the following detailed description of the invention whenconsidered in conjunction with the drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates a front view of a flexible CPAP mask in accordancewith an aspect of the present invention.

FIG. 2 illustrates a side view of the flexible CPAP mask of FIG. 1 inaccordance with an aspect of the present invention.

FIG. 3 illustrates a back view of the flexible CPAP mask of FIG. 1 inaccordance with an aspect of the present invention.

FIG. 4 illustrates a back view of another flexible CPAP mask inaccordance with an aspect of the present invention.

FIG. 5 illustrates a front view of the flexible CPAP mask of FIG. 4 inaccordance with an aspect of the present invention.

FIG. 6 illustrates a top view of the flexible CPAP mask of FIG. 4 inaccordance with an aspect of the present invention.

FIG. 7 illustrates a bottom view of the flexible CPAP mask of FIG. 4 inaccordance with an aspect of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides a-flexible mask for use in a continuouspositive airway pressure system. The present invention will now bedescribed with reference to the drawings, wherein like referencenumerals are used to refer to like elements throughout. It is to beappreciated that the various drawings are not necessarily drawn to scalefrom one figure to another nor inside a given figure, and in particularthat the size of the components are arbitrarily drawn for facilitatingthe reading of the drawings. In the following description, for purposesof explanation, numerous specific details are set forth in order toprovide a thorough understanding of the present invention. It may beevident, however, that the present invention may be practiced withoutthese specific details.

FIGS. 1-3 illustrate an example of a respiratory interface device 50 inaccordance with an aspect of the present invention. The interface device50 includes a respiratory mask 100 that interfaces with a face of apatient. The respiratory mask 100 comprises a body portion 110 thatforms an enclosure around a nose of a patient and at least one set ofheadgear strap flanges 120, 130. The body portion 110 is manufacturedfrom an elastomeric material such as polyurethane, silicone, or anyother suitable material, and can be substantially triangular in shape soas to fit the contours of a patient's face from above the nose to amustache area, located between the nose and the lips. However, it is tobe appreciated that the body portion 110 can be of any other suitableshape (e.g., circular). In contrast to conventional respiratory masks,the body portion 110 of the present invention is not coupled to or doesnot include a polycarbonate frame, or any other type of rigid shell.Instead, the entire body portion 110 is molded from an elastomericmaterial, such as silicon; thereby, providing a substantial increase incomfort to the patient.

Two sets of headgear strap flanges 120, 130 can be materially integrallymolded with the body portion 110, as depicted in FIGS. 1-3; however, itis to be appreciated that the mask 100 can include any number ofheadgear strap flanges, including one, if desired. Further, the headgearstraps can be coupled to the body portion 110 in any suitable manner.The headgear strap flanges will be described in further detail below.

The interface device 50 also includes one or more supply tubes 140coupled to the body portion 110 of the mask 100 to deliver air pressurefrom a ventilation device (not shown) to a patient. In particular, theventilation device forces a gas, such as air, through the supply tubes140 and can be provided by a continuous positive airway pressuremachine, a bi-level positive airway pressure machine, an intermittent(non-continuous) positive pressure machine, or any other suitablemachine to deliver air to the patient via the mask 100. For sleep apneatherapy, the ventilation device will usually supply room air at apressure of between five and fifteen centimeters of water. The room airmay be supplemented with oxygen if desired by splicing an oxygen supplyline into the supply hose or using a triple port connector.

A swivel component 150 can be coupled to the supply tube(s) 140 tofacilitate easy manipulation of the tubing 140 for patient comfort. Eachof the supply tubes 140 includes an end portion, which is coupled to theswivel component 150 to facilitate easy manipulation of the supply tubes140 for patient comfort. The swivel component 150 comprises asubstantially cylindrical element 152 for coupling with a tube of theventilation device and a hemispherical element 154 having two tubularengaging portions (not shown). The two tubular engaging portions areutilized for coupling with end portions of the supply tubes 140. Thecylindrical element 152 and the hemispherical element 154 are operableto swivel with respect to each other. For instance, the cylindricalelement 152 and the hemispherical element 154 can swivel about eachother by 360°. It is to be appreciated that any suitable structurecontemplated for swiveling the mask 100 with the tube of the ventilationdevice can be utilized.

Turning back to the body portion 110 of the mask 100, a bellows-likestructure (hereinafter referred to as “bellows”) 160 is integrallymolded near the mustache region of the body portion 110 to create asealing interface between a bottom portion of the mask 100 and thepatient's nose. More specifically, the sealing interface is createdbetween an inner bottom surface 162 of the mask 100 and a bottom,triangular shaped area of the nose. The bellows 160 act in a mannersimilar to a compression spring to apply a gentle upward pressure to thenose thereby holding the sealing surfaces (e.g., the inner bottomsurface 162 and the bottom area of the nose) in sealing engagement withone another. The bellows 160 is adjustable in length between acontracted state and an expanded state.

First and/or second sets of headgear strap flanges 120, 130 can bematerially integral with, or coupled to, the body portion 110, tofacilitate utilization of headgear straps (not shown). The first set ofheadgear strap flanges 120 can be located at a bottom portion of thebody 110. The second set of headgear strap flanges 130 is located at atop portion of the body 110. The flanges 120, 130 include apertures 170,180, respectively, for receiving the headgear straps. When the mask ispositioned around the nose of the patient, the headgear straps fastenaround the patient's bead and apply pressure to the body portion 110,securing the mask 100 against the patient's face. In particular, thefirst set of headgear strap flanges 120 are upwardly angled such that aheadgear strap coupled to the first set of headgear strap flanges 120applies a backwards and upwards pressure, at approximately a 45 degreeangle, to the bellows portion 160 of the mask 100. The spring-likefeature of the bellows 160 partially absorbs this upward pressure andapplies gentle pressure to the bottom the nose, thereby, forming anairtight seal between the bottom portion of the body 110 and thepatient's nose. The second set of headgear strap flanges 130 aredownwardly angled to facilitate a headgear strap applying a backwardsand downwards pressure to a top portion of the mask 100, securing thebody portion 110 against a nasal bridge region of the patient's nose.Alternatively, the mask can include only one set of headgear strapflanges, as illustrated in FIGS. 4-7.

Also extending from the body 110 of the mask are one or more air inlets165, two air inlets 165 are illustrated with respect to FIGS. 1-3. Theair inlets 165 can extend from a side portion of the body 110 in asubstantially upward direction and can be materially integral with thebody 110. For instance, one air inlet 165 can be located on each side ofthe bellows portion 160 of the body 110. It is to be appreciated thatone or more air inlets can be located anywhere on the body portion ofthe body 110 and is contemplated as falling within the scope of theinvention. The flexible air supply tubing 140 can be coupled to ormaterially integral with the air inlets 165. The tubing 140 can be madeof a relatively flexible adjustable material, such as plastic or thelike, and is employed as a conduit for ventilation.

Although not illustrated, it is to be appreciated that the respiratoryinterface device 50 can include a Y-connector (not shown) having a firstend adapted to receive a supply hose from a mechanical ventilator (notshown) and a second end having a pair of ports (not shown) withconnectors for attachment to the air supply tubing. It is to beappreciated that the Y-connector described with respect to the presentinvention can alternatively be a T-connector, or any other three-waytubing connector as is known in the art. The swivel component 150 canalso be coupled to the connector to facilitate easy manipulation of thetubing 140 for patient comfort.

As shown in FIG. 1, the tubing 140 extends for a short distance along aplane defined by the base of the mask 100 and then bends downward. As aresult, the weight and torque produced by the supply tubes 140 aresupported by at least the first set of headgear straps 120, therebydecreasing a chance of the tubing 140 disturbing the sealing means andpotentially breaking the seal between the mask 100 and the patient'sface. Alternatively, the supply tubes 140 can be looped over thepatient's ears.

Turning now to FIG. 3, a back view of the flexible CPAP mask 100 isdepicted in accordance with an aspect of the present invention. The mask100 includes a face-engaging portion 190. The face-engaging portion 190includes a nasal bridge region 200 positioned in use above the patient'snose at a bridge portion thereof and a mustache region 210 generallypositioned in use between the nares of the nose and the lips. A cheekregion 220 separates the nasal bridge region 200 and the mustache region210. The face-engaging portion 190 is flexible to accommodate aplurality of different facial contours.

I.r1 use, the patient's nose is received through an aperture 230 into achamber within the body 110 of the mask 100. The face-engaging portion190 thus contacts both a surface of the patient's nose and a portion ofthe patient's face in the mustache region between the base of the noseand the upper lip, and around the sides and over the bridge of the nose.The shape of the face-engaging portion 190 is particularly suited toseal the region of the facial contour that is the crease between thesides of the nose and the face. The nasal bridge region 200 of the mask100 can include a strengthening portion to mitigate buckling of thenasal bridge region 200 when the headgear straps apply tension on themask 100.

The mask 100 of the present invention provides an airtight seal whileeliminating the need for the rigid name employed in conventional masks.A first sealing interface is formed between a top portion of the mask100 and the patient's face. A first headgear strap fastens around thepatient's head and applies backwards pressure to the mask, securing thetop portion of the mask 100 against the patient's face. The firstheadgear strap also applies a downward pressure, at approximately a45-degree angle, to the bridge region of the patient's face, therebyforming an airtight seal between a top portion of the mask 100 and thepatient's nose. A second sealing interface is provided when a topsurface of the bellows 160 contacts the bottom, generally triangularshaped surface of the patient's nose, which includes the columella,infratip lobule, and alar sidewall portions of the nose. A secondheadgear strap fastens around the patient's head and applies backwardpressure to mask 100 securing it against the patient's mustache region.Also, the second headgear applies upward pressure, at approximately a45-degree angle, to the bellows 160. The spring-like feature of thebellows 160 partially absorbs this upward pressure and applies gentlepressure to the bottom the nose, thereby, forming an airtight sealbetween the bottom portion of the mask 100 and the patient's nose.

FIGS. 4-7 illustrate another example of a respiratory mask 250 inaccordance with an aspect of the present invention. The respiratory mask250 can be manufactured from an elastomeric material such aspolyurethane, silicone, or any other suitable material, and issubstantially triangular in shape so as to fit the contours of apatient's face from above the nose to a mustache area, located betweenthe nose and the lips. In contrast to conventional respiratory masks,the mask 250 of the present invention does not include a polycarbonateframe, or any other type of rigid shell. Instead, an entire body portion260 of me mask 250 is molded from an elastomeric material, such assilicon; thereby, providing a substantial increase in comfort to thepatient. A set of headgear strap flanges 270 can be integrally moldedwith the body portion 260.

A bellows-like structure (hereinafter referred to as “bellows”) 280 isalso integrally molded in the body portion 260 to create a sealinginterface between an inner bottom portion 285 (FIG. 6) of the mask 250and the patient's nose. More specifically, the sealing interface iscreated between the inner bottom portion 285 of the mask 250 and abottom, triangular shaped area of the nose. The bellows 280 act in amanner similar to a compression spring to apply a gentle upward pressureto the nose thereby holding the sealing surfaces (e.g., the top surfaceof the bellows 280 and the bottom area of the nose) in sealingengagement with one another. The bellows 280 is adjustable in lengthbetween a contracted state and an expanded state.

A nasal bridge portion of the mask 250 includes a notch 290 forreceiving a bridge of the patient's nose.

FIG. 7 depicts a bottom perspective view of the mask 250 in accordancewith an aspect of the present invention The mask 250 includes at leastone bleeder port 300 projecting from a bottom surface 310 of the body250. In the example illustrated in FIG. 7 two bleeder ports 300 areutilized and are axially aligned with the patient's nares whenpositioned within the inner portion of the mask 250. The bleeder ports300 can be cylindrical and have an internal diameter of about threemillimeters and a length of about 0.25 inches, for example. The internaldiameter of the bleeder ports 300 are ample to permit venting of carbondioxide exhaled by the patient while not being so large as to cause asignificant pressure drop in the interior of the mask 250. The axialalignment of the bleeder port 300 with the nares creates a direct pathfor venting of the expired gases. At substantially the same time,laminar flow of air supplied by the supply tubes is normal to thebleeder ports 300, such that air supplied by the ventilator must bendabout ninety degrees to exit through the bleeder ports 300. The effectof this construction is that the bleeder ports 300 are virtually silentin operation, mitigating a whistle noise associated with bleeder holesin conventional ventilation interfaces.

Although a detailed description of a preferred embodiment of thisinvention has been shown and described hereinabove, it will beunderstood that various modifications and rearrangements of the partsand their respective features may be resorted to without departing fromthe scope of the invention as disclosed herein.

What is claimed is:
 1. An interface device comprising: a respiratorymask comprising: a body adapted to form an enclosure around a nose of apatient, wherein the entire body is manufactured from an elastomericmaterial; and a bellows-like structure integrally molded in a mustacheregion of the body.
 2. The interface device of claim 1, wherein thebellows-like structure is adapted to create a sealing interface betweena bottom portion of the mask and a patient's nose.
 3. The interfacedevice of claim 1, wherein the body is substantially triangular in shapeso as to fit contours of a patient's face from above a nose to amustache area, located between the nose and lips.
 4. The interfacedevice of claim 1, further comprising two sets of headgear strapflanges.
 5. The interface device of claim 4, wherein the headgear strapflanges are materially integral with the body.
 6. The interface deviceof claim 4, wherein a first set of headgear strap flanges is located ata bottom portion of the body and a second set of headgear strap flangesis located at a top portion of the body.
 7. The interface device ofclaim 6, wherein the first set of headgear strap flanges is upwardlyangled and the second set of headgear strap flanges is downwardlyangled.
 8. The interface device of claim 1, further comprising one ormore supply tubes coupled to the body portion.
 9. The interface deviceof claim 8, wherein the one or more supply tubes extend for a distancealong a plane defined by a base of the mask and then bend downward. 10.The interface device of claim 8, further comprising a swivel componentcoupled to the one or more supply tubes.
 11. The interface device ofclaim 1, further comprising one or more air inlets extending from thebody.
 12. The interface device of claim 11, wherein two air inlets arematerially integral with the body such that each air inlet extends froma respective side portion of the body.
 13. The interface device of claim12, wherein the two air inlets extend in a substantially upwarddirection.
 14. A respiratory mask comprising: an elastomeric body; abellows-like structure integrally molded in a mustache region of thebody; and at least one headgear strap flange integrally molded with thebody.
 15. The respiratory mask of claim 14, wherein the body is adaptedto form an enclosure around a nose of a patient, and wherein the entirebody is manufactured from an elastomeric material.
 16. The respiratorymask of claim 14, further comprising a first set of headgear strapflanges coupled to a bottom portion of the body.
 17. The respiratorymask of claim 16, further comprising a second set of headgear strapflanges coupled to a top portion of the body.
 18. The respiratory maskof claim 17, wherein the second set of headgear strap flanges aredownwardly angled.
 19. The respiratory mask of claim 16, wherein thefirst set of headgear strap flanges are upwardly angled.
 20. Arespiratory mask comprising: elastomeric mask means for forming anenclosure around a nose of a patient; and bellows integrally molded inthe mask means for creating a sealing interface between an inner bottomportion of the mask means and a bottom portion of a patient's nose.